Variant report
Variant | rs12266990 |
---|---|
Chromosome Location | chr10:91444950-91444951 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:91443800-91445000 | Enhancers | Primary monocytes fromperipheralblood | blood |
2 | chr10:91444200-91445200 | Enhancers | Fetal Muscle Leg | muscle |
3 | chr10:91444400-91445000 | Enhancers | Osteobl | bone |
4 | chr10:91444600-91445000 | Enhancers | Monocytes-CD14+_RO01746 | blood |
5 | chr10:91444600-91445600 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
6 | chr10:91444600-91445800 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
7 | chr10:91444600-91450400 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
8 | chr10:91444600-91460800 | Weak transcription | Left Ventricle | heart |
9 | chr10:91444800-91453000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
10 | chr10:91444800-91455000 | Weak transcription | NHEK | skin |